Gene-specific Copy Number Variation Probe-ITGA7
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| Catalog: |
CNVFP-ITGA7-07667 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ITGA7). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
ITGA7 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ITGA7 genes. This product achieves the purpose of detection by hybridizing with the ITGA7 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Integrin Subunit Alpha 7 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Feb 2009] |
| Gene Symbol |
ITGA7 |
| Location |
12q13.2 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 56078353-56106089 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-ITGA7-07667-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ITGA7-07667-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ITGA7-07667-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ITGA7-07667-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ITGA7-07667-AQ |
467nm |
418nm |
|
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